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As a result of studies of subchronic toxicity of subcutaneously administered L-carnitine for veterinary use in laboratory animals, it was found that the dosage of 1/5 of the maximum tolerated, and the dosage of 1/10 of the maximum tolerated, do not cause external signs of toxicosis and death of rats
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Persistent pain or discomfort merits a pelvic exam to exclude dermatologic conditions or infection
Conjugated bilirubin triggers anemia by inducing erythrocyte death
Randomization and Group Allocation Following screening and informed consent, patients were randomized into two equal groups, with 25 participants allocated to each group
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